US9055992B2

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Publication number: US9055992B2
Application number: US14/106,555
Authority: US
Inventors: Bryan Larson
Original assignee: Individual
Current assignee: Individual
Priority date: 2012-12-14
Filing date: 2013-12-13
Publication date: 2015-06-16
Anticipated expiration: 2033-12-13
Also published as: US20140170594A1; WO2014093926A1; CA2894462A1

Abstract

A carpule for a dental syringe provides an internal piston disposed between a front septum and a rear plunger. The internal piston is hollow and includes a thin membrane front. The internal piston is designed to offer minimum resistance to movement in the carpule body to allow for aspiration and for easy dispensing. The internal piston divides the carpule into two anesthetic chambers, allowing an anesthetic without a vasoconstrictor and an anesthetic with a vasoconstrictor to be dispensed sequentially in a single injection and without causing undue trauma to the patient.

Description

PRIORITY

The present application claims the benefit of U.S. Provisional Application Ser. No. 61/737,244, filed Dec. 14, 2012, which is herein incorporated by reference in its entirety.

THE FIELD OF THE INVENTION

The present invention relates to dental anesthetic. More particularly, the present invention relates to syringe and carpule systems for delivering dental anesthetic.

BACKGROUND

Syringes are used to deliver medication. For example, syringes are used to deliver anesthetic to patients' mouths before performing dental work. Many people dislike receiving injections. Receiving injections may cause anxiety and discomfort for the person which extends beyond the pain associated with being pierced by a needle and receiving the injection. Applicant thus desires to reduce the anxiety and discomfort associated with receiving injections and in particular to improve the patient experience with dental anesthetic.

BRIEF DESCRIPTION OF THE DRAWINGS

Non-limiting and non-exhaustive examples of the present invention are described with reference to the following figures, wherein like reference numerals refer to like parts throughout the various views unless otherwise specified.

FIG. 1 shows a dental syringe and a carpule for the syringe.

FIG. 2 shows a more detailed partially cut-away view of the carpule.

FIG. 3 shows a rear perspective view of the carpule.

FIG. 4 shows a front perspective view of the carpule.

FIGS. 5 through 11 show cross sectional views of the carpule.

FIG. 12 shows a side view of the carpule.

FIG. 13 shows a front view of the carpule.

FIG. 14 shows a back view of the carpule.

Corresponding reference characters indicate corresponding components throughout the several views of the drawings. Skilled artisans will appreciate that elements in the figures are illustrated for simplicity and clarity and have not necessarily been drawn to scale. For example, the dimensions of some of the elements in the figures may be exaggerated relative to other elements to help to improve understanding of various examples of the present invention. Also, common but well-understood elements that are useful or necessary in a commercially feasible embodiment are often not depicted in order to facilitate a less obstructed view of these various embodiments of the present invention.

It will be appreciated that the drawings are illustrative and not limiting of the scope of the invention which is defined by the appended claims. The examples shown each accomplish various different advantages. It is appreciated that it is not possible to clearly show each element or advantage in a single figure, and as such, multiple figures are presented to separately illustrate the various details of the examples in greater clarity. Similarly, not every example need accomplish all advantages of the present disclosure.

DETAILED DESCRIPTION

In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. It will be apparent, however, to one having ordinary skill in the art that the specific detail need not be employed to practice the present invention. In other instances, well-known materials or methods have not been described in detail in order to avoid obscuring the present invention.

Reference throughout this specification to “one embodiment”, “an embodiment”, “one example” or “an example” means that a particular feature, structure or characteristic described in connection with the embodiment or example is included in at least one embodiment of the present invention. Thus, appearances of the phrases “in one embodiment”, “in an embodiment”, “one example” or “an example” in various places throughout this specification are not necessarily all referring to the same embodiment or example. Furthermore, the particular features, structures or characteristics may be combined in any suitable combinations and/or sub-combinations in one or more embodiments or examples. In addition, it is appreciated that the figures provided herewith are for explanation purposes to persons ordinarily skilled in the art and that the drawings are not necessarily drawn to scale.

Embodiments in accordance with the present invention may be embodied as an apparatus or method. Accordingly, the present invention may take the form of an embodiment combining structural or method aspects that may all generally be referred to herein as a “system.”

The disclosure particularly describes how to reduce patient pain and discomfort while administering anesthetic. Particularly, the present disclosure describes how a syringe and carpule system may be used to sequentially deliver different types of anesthetic.

Local anesthetic is frequently used for dental work such as fillings and the like. Typically, an anesthetic is applied to a region of the mouth by injecting the anesthetic into the soft tissue of the mouth with a syringe. Many local anesthetics used in dentistry, however, are vasodilators. These anesthetics cause dilation of blood vessels and an increase in blood flow in the area around the injection. This dilation of blood vessels removes the anesthetic from the injection area more quickly and reduces the effective duration of the anesthetic. These anesthetics are often unsuitable as they have insufficient duration for a dental procedure.

Some dental anesthetics contain epinephrine. The epinephrine is a vasoconstrictor and reduces blood flow in the anesthetized area, prolonging the effect of the anesthetic. Epinephrine, however, decomposes and requires a preservative to remain effective. The preservative causes the anesthetic to become acidic and causes pain on contact with tissue. Patients thus endure some pain until the anesthetic begins to function. This increases the discomfort and anxiety of the patient.

To decrease the pain, two different anesthetics may be used. A first anesthetic which does not contain a vasoconstrictor and preservative may be used. This first anesthetic may be used to numb the area even though the numbing effect may be short lived due to the dilating effect of the anesthetic. The first anesthetic may be used to numb the area sufficiently to allow the dentist to inject a second anesthetic with a vasoconstrictor and preservative. Many people, however, have an aversion to the syringe needle and would not want multiple injections even if it would decrease the pain and discomfort of the anesthetic.

Accordingly, a syringe system may be used which sequentially dispenses two different anesthetics in a single injection. In this manner, a dentist may dispense the first anesthetic, wait a moment if desired, and continue with dispensing the second anesthetic. All of this may be performed without withdrawing the syringe from the patient, minimizing the patient's discomfort with the procedure. A prefilled carpule may be provided which has a first anesthetic chamber and a separate second anesthetic chamber so that a dentist may dispense the two anesthetics sequentially.

Turning now toFIG. 1, a dental syringe and an anesthetic carpule are shown. Thedental syringe10 is reusable and thecarpule58 is disposable. Thesyringe10 includes asyringe body14 with anopening18. Thesyringe body14 may be tubular in nature, and may be formed from steel tube or rolled metal. Theopening18 is approximately the same width as the internal cavity of thesyringe body14. Asyringe plunger22 extends into thebody14 and is movable along the length of the body. The distal end of theplunger22 includes aharpoon26. The proximal end of thesyringe10 has ahandle portion30 which may include laterally extendingflanges34 forming finger grips which are attached to thebody14. The proximal end of thesyringe10 may include other types of finger grips. Thesyringe10 also typically includes athumb grip38 attached to theplunger22. Thethumb grip38 may be formed in a ring shape, allowing controlled aspiration and dispensing form thesyringe10. Thehandle portion30 andthumb grip38 allow a dentist to easily grasp and manipulate thesyringe10 during use. The distal end of thesyringe10 includes aneedle adapter40. Theneedle adapter40 often is a threaded adapter to which ahypodermic needle42 may be attached.

Aneedle42 is attached to the distal end of thesyringe body14. Theneedle42 may be disposable. Theneedle42 includes an elongate and sharpened external hypodermic needle46 (the injection end of the needle) formed of thin tubing, an attachment collar orhub50, and acartridge end54 of the needle which is typically sharpened and which extends proximally from theneedle hub50. The cartridge end of theneedle54 and injection end of theneedle46 are often created from a single piece of hypodermic tubing to which ahub50 is attached. Accordingly, the lumen of the injection end of theneedle46 is connected to the lumen of the cartridge end of theneedle54. Theneedle hub50 may be threaded or have another fitting to allow theneedle42 to be removably attached to theneedle adapter40 on the distal end of thesyringe body14.

A carpule58 contains anesthetic and is used with thesyringe10 to dispense anesthetic. Acarpule58 may be a prefilled and disposable anesthetic cartridge. Adisposable carpule58 provides sterility and convenience of use without excessive cost. Thecarpule58 includes a hollow tubular glass body/cartridge62. The distal end of thecarpule body62 is formed with areduced diameter neck64 and a circumferential ridge/bead60 which is larger in diameter than the neck. Thebody62 is closed at the distal end with aseptum66 and a crimpedcap70 attaching the septum to the body. The septum attaches to the distal face of thebody62 and the cap extends over part of the septum, and over thebead60. Thebody62 is tubular between theneck64 and the proximal end of the body.

Asilicone rubber plunger74 is disposed in the bore of thebody62 and seals the proximal end of the body. Theplunger74 is typically made of an elastomeric material such as silicone, rubber, etc. An internal floatingpiston78 divides the interior lumen/bore of thecarpule body62 into a firstanesthetic chamber82 and a secondanesthetic chamber86. The firstanesthetic chamber82 is located between theseptum66 and thepiston78 and the secondanesthetic chamber86 is located between thepiston78 and theplunger74. Thecarpule58 is typically provided prefilled with a first anesthetic in the firstanesthetic chamber82 and a second anesthetic in the secondanesthetic chamber86. In one example, thecarpule58 may be provided with a first medicine in thefirst chamber82 and a second medicine in thesecond chamber86. The first medicine may be an anesthetic and the second medicine may be a drug or vaccine, as an example.

In use, thecarpule58 is inserted through theopening18 and into the interior of thesyringe body14. Theopening18 is slightly larger than the carpule58 to allow the carpule to be loaded into the syringe. Theharpoon26 is inserted into theplunger74 of thecarpule58. Theharpoon26 is typically barbed or hook shaped and becomes reliably engaged with theplunger74 so that it is not accidentally withdrawn therefrom if the syringe is used for aspiration. Thecarpule58 is placed at the forward/distal end of thesyringe body14. Theseptum66 is pierced with thecartridge end54 of theneedle42, causing thecartridge end54 theneedle42 to pierce theseptum66 and enter the firstanesthetic chamber82.

FIG. 2 shows an enlarged, partially cut-away drawing of the carpule58 with some parts of the syringe showing. Thecartridge end54 of theneedle42 can be seen; illustrating how thecartridge end54 of the needle may extend into theneck64 of thecarpule body62. It can also be seen how theplunger74 may be formed withribs76 to assist in sealing against thecarpule body62. Similarly, thepiston78 may be formed withribs80 to seal between thepiston78 and thecarpule body62.

FIGS. 3 and 4 show perspective drawings of thecarpule58 and assist in visualizing the various structures and components discussed herein.FIG. 3 shows a rear perspective view of thecarpule58 andFIG. 4 shows a front perspective view of the carpule. As can be seen inFIG. 4, the center of theseptum66 may be marked with anindicator68. Theindicator68 may be a small dot or circle, a raised ring, a small depression, a bump, etc. Theindicator68 may assist a user in piercing the center of theseptum66 with thecartridge end54 of theneedle42 while assembling thesyringe10. This may reduce the likelihood of any malfunction while dispensing anesthetic from thecarpule58.

FIG. 5 shows the carpule58 in cross section. Theplunger74 is cylindrical and has an outer diameter slightly larger than the bore of thebody62 so that the plunger seals against the bore. In some examples,ribs76 maybe formed around the outside of the larger body portion of the plunger to assist in sealing against the body bore and to permit smooth movement of theplunger74 within thebody62. Some features such as theribs76 shown inFIG. 2 are not shown in other figures in order to not obscure the clarity of the drawings. If desired, the distal end of theplunger74 may be formed with a reduced diameter or with a tapering or conical shape. This may be useful in allowing thecarpule58 to be filled without retaining air bubbles. Although not necessary, the distal end of theplunger74 may taper in size or be otherwise shaped to nest somewhat into the proximal end of thepiston78. The proximal end of theplunger74 is typically flat, allowing theplunger74 to receive theharpoon26. Theplunger74 is often made of an elastomer and is typically solid. Theplunger74 is sufficiently soft to receive theharpoon26.

Theseptum66 is relatively thin and is often made of rubber which may be easily pierced by theneedle42 and reliably seal against the needle during use. Theseptum66 is held against the front of thebody62 by the crimped oncap70. Additionally, adhesive may be used to seal the septum against thebody62. As can be seen inFIG. 4, theseptum66 may be manufactured with a marking68 such as a small depression, a raised circle, a printed circle, a printed center dot or cross, etc. to assist a person with placing the needle42 (thecartridge end54 of the needle in particular) through the center of the septum. Placing theneedle42 through theseptum66 closely to the center may ensure that thepiston78 functions properly as described.

Thepiston78 is generally hollow. Thepiston78 may be formed from abody portion90 and amembrane94. Thebody portion90 of thepiston78 may be formed from a sufficiently rigid elastomer or a polymer or plastic material, allowing the body portion to be structurally sound while allowing a hollow interior. Thebody portion90 is generally cylindrical with a hollow interior and may have a protrudingdistal end92 with a reduced diameter to nest within the distal end (neck64) of thecarpule body62. In many examples, thecartridge end54 of theneedle42 extends sufficiently to pierce thecartridge septum66, but does not extend into the main portion of thebody62 of the carpule. As such, themembrane94 may need to move into the neck of the carpule58 as the first anesthetic is dispensed, allowing thecartridge end54 of theneedle42 to pierce themembrane94 and allow the second anesthetic to be dispensed. Accordingly, thedistal end92 of thepiston78 may be cylindrical and hollow and may be formed with an outer diameter which is less than the inner diameter of theneck64 of thecarpule body62.

Thus, thepiston78 may have a proximal body portion which is cylindrical and which is slightly larger in diameter than the bore of thecarpule body62 and a distal body portion which is a smaller diameter. The proximal and distal body portions of thepiston78 are hollow and are open from the proximal end of thepiston78 up to themembrane94. The proximal and distal body portions are of sufficient annular thickness to support the shape of the piston and to seal against the bore of thecarpule body62. Thus, the body portion of thepiston78 may have cylindrical walls which are between about 0.015 and about 0.04 inches thick (between about 0.3 mm and 1 mm), and more commonly between about 0.02 and about 0.03 inches thick (between about 0.5 mm and 0.75 mm). Thebody90 of thepiston78 may have ribs (80,FIG. 2) which assist in sealing against the bore of thecarpule body62. These ribs may often be between about 0.001 and about 0.02 inches tall and wide (between about 0.025 mm and 0.5 mm), and may more commonly be between about 0.01 and 0.015 inches tall and wide (between about 0.25 mm and 0.35 mm). The use ofribs80 may improve the sealing while permitting smooth sliding movement of thepiston78.

Theribs80 may thus extend circumferentially around the outer diameter of thepiston78. These ribs provide a slight interference fit with the internal bore of thecarpule body62 to seal between thepiston78 and the body. The amount of interference is small, and in some examples, the ribs may be between about 0.002 and about 0.004 inches (between about 0.05 mm and 0.1 mm) larger in diameter than the bore of thecarpule body62. The amount of interference is small so that thepiston78 does not provide significant resistance to movement and does not create any significant pressure differential across themembrane94.

Thebody90 of thepiston78 may be formed from a polymer, thermoplastic, thermoplastic elastomer, etc. In on example, thebody90 of the piston may be formed from a composite of two materials. Thebody90 may be formed from a rigid thermoplastic or thermoplastic elastomer with ribs overmolded or otherwise formed from a softer elastomer or thermoplastic elastomer. This may allow thebody90 to have sufficient structural strength while remaining hollow and may allow the body/ribs to seal against the bore of thecarpule body62 reliably without causing undue resistance to thepiston78 sliding within the bore of thecarpule body62.

The distal face of thepiston78 is formed by amembrane94. Themembrane94 may be formed from a thin rubber or silicone, a thin plastic/polymer, a film such as Mylar, etc. In one example, themembrane94 may be formed from Mylar, a polyolefin such as polyethylene or polypropylene, a metal foil such an aluminum foil, etc. Themembrane94 may be between about 0.0001 and about 0.025 inches thick (between about 0.002 mm and 0.65 mm), and may typically be between about 0.0001 and 0.01 inches thick (between about 0.002 mm and 0.2 mm), or between about 0.005 and about 0.01 inches thick (between about 0.1 mm and 0.2 mm). As such, themembrane94 typically does not provide significant strength to theinternal piston78 and thebody90 of thepiston78 typically must provide all of the strength. More importantly, themembrane94 does not provide a significant resistance to puncture. As such, themembrane94 is easily punctured by thecartridge end54 of theneedle42 when moved against the needle. Themembrane94 may often be glued or heat sealed to thebody90 of theinternal piston78. Thebody90 andmembrane94 may be made as a one piece structure in some configurations. Thebody90 andmembrane94 together form a sealed and non-permeable piston that prevents fluid from the firstanesthetic chamber82 from mixing with fluid in the secondanesthetic chamber86.

FIG. 6 also shows the carpule58 in cross section. Thecarpule58 has been placed into thesyringe10 and theharpoon26 has been inserted into theplunger74. As shown, thecartridge end54 of theneedle42 is inserted through thecarpule septum66 and theneedle42 is attached to theneedle adapter40. As seen, thecartridge end54 of theneedle42 often does not extend beyond the distal neck of thecarpule58. In this situation, thedistal end92 of thepiston78 should be reduced in diameter so that it can move into the carpule neck and thecartridge end54 of theneedle42 can pierce themembrane94.

In use, theharpoon26 allows theplunger74 to be moved distally in the carpule to dispense anesthetic and proximally in the carpule to aspirate.FIG. 7 illustrates the use of the carpule58 in aspiration. When the injection end46 of theneedle42 is placed into the patient for an injection, theplunger22 may be withdrawn slightly to aspirate or cause a reduced pressure within thecarpule58. This will show if theneedle42 is placed in a blood vessel as, in such a location, a small amount ofblood98 is drawn into thecarpule58 through theneedle42. The freely movinginternal piston78 allows a dentist to do so as it does not provide sufficient resistance to movement which would make this task more difficult. To ensure that aspiration with thecarpule58 is possible, it is typically desirable that thepiston78 will move freely within the bore of thecarpule body62 with an applied pressure of 10 psi or less. More preferably, thepiston78 will move freely within thecarpule body62 under a pressure of 5 psi or less. After the aspiration check demonstrates that theneedle46 is properly positioned (i.e. not within a blood vessel), the dentist may proceed to dispense anesthetic.

Thecarpule58 may include afirst anesthetic102 without a vasoconstrictor in the firstanesthetic chamber82 and may include a seconddifferent anesthetic106 with a vasoconstrictor and preservative in the secondanesthetic chamber86. In one example, the firstanesthetic chamber82 may be filled with an anesthetic102 such as prilocaine (such as a 4 percent solution of prilocaine), lidocaine (such as a 2 percent solution), or mepivicaine (such as a 3 percent solution) without a vasoconstrictor or a preservative. The secondanesthetic chamber86 may be filled with asuitable anesthetic106 such as lidocaine or articaine with a vasoconstrictor such as epinephrine or norepinephrine and a preservative. The firstanesthetic chamber82 may contain a smaller volume of anesthetic than the secondanesthetic chamber86. In one example, the firstanesthetic chamber82 may contain between about 10 percent and about 35 percent of the volume of the carpule58 with the secondanesthetic chamber86 containing between about 65 percent and about 90 percent of the volume of thecarpule58. In another example, the firstanesthetic chamber82 may contain between about 20 percent and about 25 percent of the volume of the carpule58 with the secondanesthetic chamber86 containing between about 75 percent and about 80 percent of the volume of thecarpule58.

FIG. 8 shows thecarpule58 while dispensing anesthetic therefrom. Theplunger74 is moved distally (by moving the syringe plunger22) to dispense some of thefirst anesthetic102 from the firstanesthetic chamber82 after placing the injection end46 of theneedle42 in a desired location within the patient. Thefirst anesthetic102 is typically an anesthetic without a vasoconstrictor such as prilocaine. This anesthetic102 allows the dentist to numb an area of the patient's mount with an anesthetic which does not cause pain. The dentist may thus slowly dispense some or all of thefirst anesthetic102 and then wait for a few seconds for thefirst anesthetic102 to take effect before dispensing thesecond anesthetic106. The complete injection may be performed without withdrawing the needle and puncturing the tissue a second time.

Where thefirst anesthetic102 does not have a vasoconstrictor, it may have a shorter useful duration than thesecond anesthetic106. As such, it may not contribute as much to the available time to perform a dental procedure. The volume of thefirst anesthetic102 is thus often minimized; providing only a sufficient amount offirst anesthetic102 to numb an area of the patient's mouth sufficiently that the patient does not feel pain upon introduction of thesecond anesthetic106. In one example, thesecond anesthetic106 may have a somewhat higher amount of vasoconstrictor than would be otherwise used to offset the amount of vasoconstrictor not present in thefirst anesthetic102. In this example, the vasoconstrictor may achieve a desired reduction in blood flow to prolong the effectiveness of thefirst anesthetic102 andsecond anesthetic106 and provide sufficient duration.

As shown, thepiston78 moves forwards as thefirst anesthetic102 is dispensed. The advancement of theplunger74 displaces thesecond anesthetic106, causing movement of thepiston78 and displacement of thefirst anesthetic102. Thefirst anesthetic102 is dispensed and thepiston78 is advanced until themembrane94 is pressed against thecartridge end54 of theneedle42 and punctured thereby. Themembrane94 is thin and easily pierced by the end of theneedle42. As such, piercing themembrane94 with theend54 of theneedle42 requires minimal force and provides minimal pressure change or disruption to the position of thesyringe10 and movement of theplunger22. This assists in the prevention of pain and trauma to the injection site from the rapid tissue expansion which may occur if thepiston78 were more difficult to pierce and a greater amount of force against theplunger74 was required, as the additional applied force would quickly dispense a volume of anesthetic once thepiston78 was pierced.

Once thecartridge end54 of theneedle42 pierces themembrane94, the secondanesthetic chamber86 andsecond anesthetic106 are exposed to the needle lumen and available for dispensing into the patient. The dentist will typically dispense thefirst anesthetic102 slowly and wait a short period of time to allow the patient's mouth to become numb. At this point, the patient will not feel discomfort while the dentist dispenses thesecond anesthetic106 which typically contains a vasoconstrictor and preservative. The vasoconstrictor may promote the longevity of both thefirst anesthetic102 and thesecond anesthetic106.

As shown inFIG. 9, theplunger74 may be move distally in thecarpule58 to dispense thesecond anesthetic106 therefrom. Thesecond anesthetic106 may be dispensed from thecarpule58 until theplunger74 is contacting thepiston78 and thepiston78 is contacting theneck64 or distal end of thecarpule body62. At this point, no further anesthetic may be dispensed.

Although some anesthetic capacity is lost in thecarpule58 due to the presence of thepiston78, the loss in capacity is small. Thecarpule58 may be about 2.5 inches long (about 63 mm) and the larger proximal portion of thepiston body90 may be about ⅛ of an inch long. This scenario would provide a carpule58 with a loss of approximately 5 percent or less of anesthetic volume.

Various processes may be used to fill or otherwise manufacture acarpule58. By way of example, one process may begin with an emptyglass carpule body62 with the open proximal end facing up. Thepiston78 may be inserted into thebody62 such that the depth from the proximal end of the body to thepiston78 allows for the desired total volume of secondanesthetic solution106 in thesecond chamber86. That is to say that thepiston78 may be placed at a location in thecarpule body62 where the volume in the carpule body lumen/bore between thepiston78 and the proximal end of thecarpule body62 is equal to the desired volume ofsecond anesthetic106. The second anesthetic chamber86 (the proximal portion of the carpule body62) may then be filled to the top with the desired secondanesthetic solution106. Theplunger74 may then be inserted into the proximal end of thecarpule body62. Inserting theplunger74 will displace the secondanesthetic solution106 in the secondanesthetic chamber86 and move thepiston78 distally as theplunger74 is pressed in place. This may be accomplished such that there is no air trapped in thesecond chamber86.

As is shown inFIGS. 1,2,4,10, and11, the distal end of theplunger74 may be manufactured with a flat distal face of with a protruding nub, point, cone, etc. The distal protrusion may be formed with a slight taper, such as a 6-8 degree taper, or with a relatively short and steeply sloped conical shape to encourage air bubbles to move away from theplunger74 and out of thebody62 when inserting the plunger into thebody62. Air bubbles may tend to move around theplunger74 and escape from the secondanesthetic chamber86 rather than becoming trapped against a flat distal face of aplunger74. Alternatively, a flat face may be easily used by filling anesthetic into the carpule body until the surface of the anesthetic liquid is level with or slightly above the proximal end of thecarpule body62. After theplunger74 is inserted to the desired depth, the secondanesthetic chamber86 is closed and sealed.

Thecarpule58 may then be inverted so that the distal end of thebody62 is facing up. The remaining empty volume inside of thebody62 will now reflect the desired volume ofanesthetic solution102 to be placed in the firstanesthetic chamber82. The firstanesthetic chamber82 may be filled with the desired firstanesthetic solution102, such as prilocaine. The firstanesthetic chamber82 is typically filled to the distal end of thecarpule body62 and any bubbles are removed from the firstanesthetic chamber82. Aseptum66 may then be placed on the distal end of thecarpule58 without trapping air bubbles in thecarpule58 and theseptum66 may be sealed to thebody62 if necessary. A collar/cap70 may be crimped in place around theseptum66 and thedistal ridge60 andneck64 of thecarpule body62. In this manner, thecarpule58 may be filled without trapping air bubbles in the carpule. If desired, thecarpule58 may be filled or treated under vacuum conditions to assist in eliminating bubbles from the carpule. Thecarpule58 may then be sterilized and packaged for use.

FIG. 12 shows a side view of thecarpule58. As the carpule is typically round and symmetrical, this view also shows the left and right sides and the top and bottom sides of the carpule.FIG. 13 shows a front view of the carpule.FIG. 14 shows a back view of the carpule.

Thecarpule58 is advantageous as it allows for minimizing pain and damage to a patient's mouth during application of anesthetic. The patient is able to receive a long lasting anesthetic without the stinging or unpleasant feeling which is typically associated with the anesthetic. The dentist is able to accomplish a comfortable and long lasting anesthesia in a smooth and easy manner which does not require multiple injections. Additionally, thecarpule58 is compatible with existing dental syringes. No change in equipment is required to implement, distribute, and use thecarpule58. The techniques for dispensing anesthetic from thecarpule58 are sufficiently similar to those techniques already used by dentists and minimal training is necessary to use the carpule.

The above description of illustrated examples of the present invention, including what is described in the Abstract, are not intended to be exhaustive or to be limitation to the precise forms disclosed. While specific examples of the invention are described herein for illustrative purposes, various equivalent modifications are possible without departing from the broader scope of the present claims. Indeed, it is appreciated that specific example dimensions, materials, voltages, currents, frequencies, power range values, times, etc., are provided for explanation purposes and that other values may also be employed in other examples in accordance with the teachings of the present invention.

Claims

What is claimed is:

1. A dental carpule comprising:

a tubular carpule body having a cylindrical bore along a length thereof, the carpule having a neck formed on a distal end thereof and a hole formed through the neck which is smaller in diameter than the bore and which connects the bore to a distal face of the carpule body;

a septum fixedly attached to the distal face of the carpule body to close the distal end of the carpule body;

a plunger disposed in a proximal end of the bore such that the plunger seals against the bore to close the proximal end of the bore;

a piston disposed in the bore between the septum and the plunger such that the piston divides the bore into a first anesthetic chamber and a second anesthetic chamber, wherein the piston comprises a generally cylindrical piston body having a hole therethrough, the hole being disposed in alignment with the bore of the carpule body and a membrane which is thin compared to a cylindrical wall of the piston body and which is attached to a distal face of the piston body to close the hole through the piston body;

wherein the piston comprises a proximal body portion which is cylindrical and which seals against the carpule body bore and a generally cylindrical distal body portion extending distally from the proximal body portion which is smaller in diameter than the proximal body portion and which is smaller in diameter than the hole through the carpule body neck;

a first anesthetic without a vasoconstrictor disposed in the first anesthetic chamber; and

a second anesthetic with a vasoconstrictor disposed in the second anesthetic chamber.

2. The carpule ofclaim 1, wherein the piston comprises ribs formed around the piston body to seal against the carpule body bore.

3. The carpule ofclaim 1, wherein the membrane is formed from a different material than the piston body.

4. The carpule ofclaim 1, wherein the cylindrical wall of the piston body has a thickness which is multiple times thicker than a thickness of the membrane.

5. A system comprising the carpule ofclaim 1, wherein the carpule is inserted into a syringe for use, and wherein an injection needle is attached to the syringe such that a cartridge end of the needle pierces the septum, and wherein the cartridge end of the needle does not extend proximally in the carpule body beyond the neck.

6. The carpule ofclaim 1, wherein the piston body is generally rigid.

7. The carpule ofclaim 1, wherein the piston is movable to a distal end of the bore and is prevented from moving further distally at the distal end of the bore, and wherein the bore is smooth along its length to the distal end.

8. A dental system comprising:

a dental carpule comprising:

a second anesthetic with a vasoconstrictor disposed in the second anesthetic chamber;

wherein the carpule is inserted into a syringe for use, and wherein an injection needle is attached to the syringe such that a cartridge end of the needle pierces the septum, and wherein the cartridge end of the needle does not extend proximally in the carpule body beyond the neck; and

wherein the membrane is smaller than the hole through the carpule neck and wherein, during use, the piston is displaced distally while dispensing the first anesthetic until the membrane passes into the carpule neck and the membrane is pierced by the cartridge end of the needle.

9. The system ofclaim 8, wherein, after the membrane is pierced by the needle, further distal advancement of the plunger dispenses the second anesthetic through the needle.

10. The carpule ofclaim 1, wherein the septum comprises an indicator mark on the center of a distal face of the septum.

11. A carpule comprising:

a tubular carpule body having a cylindrical bore disposed along a length thereof;

a septum fixedly attached to a distal end of the carpule body to seal the distal end of the carpule body;

a generally rigid piston disposed in the bore between the septum and the plunger such that the piston divides the bore into a first medicine chamber and a second medicine chamber;

wherein the piston comprises a generally cylindrical piston body having a hole therethrough, the hole being disposed in alignment with the bore of the carpule body, and a membrane attached to a distal face of the piston body to close the hole through the piston body, the hole extending through the piston body to expose a proximal face of the membrane;

wherein the piston more specifically comprises a generally cylindrical proximal piston body, a shoulder disposed at the distal end of the proximal piston body, and a generally cylindrical distal body section which has a diameter which is smaller than a diameter of the proximal piston body and which protrudes distally from the shoulder, and wherein the distal body section is nestable within a reduced diameter carpule body neck which extends distally from the bore, and wherein the membrane is attached to a distal face of the distal body section;

a first medicine disposed in the first medicine chamber; and

a second medicine different than the first medicine disposed in the second medicine chamber.

12. The carpule ofclaim 11, wherein the piston is movable to the distal end of the bore and is prevented from moving further distally at the distal end of the bore, and wherein the distal end of the bore is smooth.

13. A system comprising the carpule ofclaim 11, wherein, during use of the carpule, a needle is inserted through the septum and into the carpule body such that the needle remains in the carpule body neck, the plunger is advanced, causing advancement of the piston and dispensing of the first medicine until the membrane is pushed into the carpule body neck and against the needle and the needle punctures the membrane, and subsequent advancement of the plunger dispenses the second medicine.

14. A carpule comprising:

a carpule body having a bore along a length thereof;

a pierceable seal attached to a distal end of the carpule body to close a distal end of the bore;

a plunger disposed in a proximal end of the bore to close the proximal end of the bore, the plunger being slidable within the bore;

a piston disposed in the bore between the seal and the plunger, the piston sealing against the bore to divide the bore into a first medicine chamber and a second medicine chamber;

wherein the piston comprises a cylindrical body, a membrane disposed on a distal end of the cylindrical body, and an opening in a proximal end of the cylindrical body, the opening extending distally to the membrane such that the membrane is exposed to the proximal end of the piston;

wherein the distal end of the carpule body has a neck having a reduced diameter hole therethrough and wherein a distal portion of the piston body is generally cylindrical and has a reduced diameter which permits the distal portion of the piston body and the membrane to extend into the carpule body neck;

wherein the piston has a range of distal movement which terminates adjacent a distal end of the bore, and wherein the bore is smooth throughout said range of distal movement;

a first liquid medicine disposed in the first medicine chamber; and

a second liquid medicine different from the first medicine disposed in the second medicine chamber.

15. The carpule ofclaim 14, wherein the piston body comprises a cylindrical wall, and wherein the membrane is thin compared to the cylindrical wall.

16. The carpule ofclaim 14, wherein the first medicine is an anesthetic without a vasoconstrictor and the second medicine is an anesthetic with a vasoconstrictor.

17. The carpule ofclaim 14, wherein the piston cylindrical body is generally rigid.